Dupuis-Williams P, Klotz C, Mazarguil H, Beisson J
Centre de Génétique Moléculaire, Associé à l'Université Pierre et Marie Curie, Gif-sur-Yvette, France.
Biol Cell. 1996;87(1-2):83-93. doi: 10.1016/s0248-4900(97)89840-1.
The ciliated protozoan Paramecium harbours a particularly large diversity of microtubule networks, ranging from the elaborate and stable ciliary axonemes and basal bodies to very dynamic cytoplasmic, cortical or intranuclear arrays. Their organization and individual cycle of assembly/disassembly are well known and extensive immunocytochemical studies of the post-translational modifications in the various microtubule systems have been reported. However, in order to better understand the biogenesis of these multiple and diverse microtubule arrays, it seemed necessary to characterize the tubulin gene family. We show that P tetraurelia possesses four alpha- and three beta-genes and we report the cloning and sequencing of two intronless alpha-genes, alpha PT1 and alpha PT2, which code for very similar polypeptides, differing only by their unusual C-terminal amino acids, respectively GLY and ALA. Partial sequencing of the two other alpha-genes suggests an absence of any further isotype diversity. In an attempt to study the expression of alpha PT1 and alpha PT2, polyclonal antibodies were raised against the twelve C-terminal amino acids corresponding to the deduced polypeptide sequences. The reactivity of these anti-sequence antibodies was studied on blots of soluble tubulin and in situ and compared with that of other well characterized anti-alpha-tubulin antibodies. The molecular data show that in Paramecium, like in other ciliates, microtubule diversity does not arise from tubulin isotype diversity. The immunocytological data indicate that the native C-terminal sequences are predominantly detected in transient or nascent microtubule arrays and lead us to propose: 1) that the C-terminal TYR, absent in Paramecium and in most cilate species, has no intrinsic functional role; and 2) that post-translational modifications do not seem directly instrumental in the geometry and functions of microtubule arrays.
纤毛原生动物草履虫拥有特别多样的微管网络,从精细且稳定的纤毛轴丝和基体到非常动态的细胞质、皮层或核内微管阵列。它们的组织以及组装/拆卸的个体循环是众所周知的,并且已经报道了对各种微管系统中翻译后修饰的广泛免疫细胞化学研究。然而,为了更好地理解这些多样的微管阵列的生物发生,表征微管蛋白基因家族似乎是必要的。我们表明四膜虫拥有四个α基因和三个β基因,并且我们报道了两个无内含子的α基因αPT1和αPT2的克隆和测序,它们编码非常相似的多肽,仅在其不寻常的C末端氨基酸上有所不同,分别为GLY和ALA。另外两个α基因的部分测序表明不存在任何进一步的同型多样性。为了研究αPT1和αPT2的表达,针对与推导的多肽序列相对应的十二个C末端氨基酸产生了多克隆抗体。研究了这些抗序列抗体在可溶性微管蛋白印迹上以及原位的反应性,并与其他特征明确的抗α微管蛋白抗体的反应性进行了比较。分子数据表明,在草履虫中,与其他纤毛虫一样,微管多样性并非源于微管蛋白同型多样性。免疫细胞学数据表明,天然C末端序列主要在瞬时或新生微管阵列中被检测到,并使我们提出:1)在草履虫和大多数纤毛虫物种中不存在的C末端酪氨酸没有内在功能作用;2)翻译后修饰似乎并非直接有助于微管阵列的几何形状和功能。